Canonical Allele Identifier: CA2686252317
Gene: FGF20 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.16992799del , CM000670.2:g.16992799del GRCh38
NC_000008.10:g.16850308del , CM000670.1:g.16850308del GRCh37
NC_000008.9:g.16894679del NCBI36
NG_015978.1:g.14368del

Transcript Alleles

HGVS Amino-acid change
ENST00000180166.6:c.*274del MANE Select ENSP00000180166.5:n.*274del
ENST00000180166.5:c.*274del ENSP00000180166.5:n.*274del
NM_019851.3:c.*274del MANE Select NP_062825.1:n.*274del